ODCs

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6 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 3

1 OMIM reference -
1 associated gene
No signs/symptoms info

Fetal and neonatal alloimmune thrombocytopenia

Von Willebrand disease type 2B


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GP1BA ITGA2B ITGB3	(0.89) (0.55) (0.52)	VWF VWF VWF

Citations in the biomedical literature:

Fetal and neonatal alloimmune thrombocytopenia		Von Willebrand disease type 2B
	Synonym(s): - NAIT		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare hematologic disease		Classification (Orphanet): - Rare genetic disease - Rare hematologic disease

	Classification (ICD10): - Certain conditions originating in the perinatal period -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.